Nadine S. Kurz

FusionPath predicts gene fusion pathogenicity using protein structural data and contextual embeddings, outperforming existing methods with AUC scores of 0.95 and 0.87.

AstraKit provides a unified KNIME workflow suite for precision medicine analytics, integrating variant interpretation, multi-omics analysis, and drug response modeling.

PanCNV-Explorer integrates and normalizes copy number variation data across 33 cancer types to provide a unified resource for analyzing CNV frequency and functional impact.

AdaGenes processes and filters sequence variant data from WES/WGS efficiently, enabling scalable and interactive analysis for genomics applications.

TCRanalyzer provides a user-friendly tool for analyzing TCR diversity, clonal expansion, and antigen specificity across tumor datasets.

PriOmics integrates proteomics with other omics data using graphical models to better understand relationships between proteins and their modifications.